FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 3062577 · Received March 16, 2013

Report

Report Number
1824206-2013-01478
Event Type
Malfunction
Date Received
March 16, 2013
Date of Event
February 16, 2013
Report Date
February 16, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THAT THE PATIENT PENDANT WIRES ARE EXPOSED. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
111592 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

Patients

Seq Age Sex Outcome Treatment
1